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Emergent exotic phenomena in the self-assembled process of vertically aligned nanocomposite (VAN) thin film remain under intensive studies. Insight exploration on the self-assembled formation from the combination of two different phases of materials is not only important to optimize the physical properties yields from those combined materials, but also open up a new avenue to discover new materials with the VAN system. In this work, the thermodynamic control of the self-assembled formation of BiFeO3-CoFe2O4 (BFO-CFO) VAN thin film has been confirmed by studying the effects of substrate temperature during the growth process by pulsed laser deposition (PLD) technique. The structural examination results on the samples, which were growing with various substrate temperatures highlight the importance of the thermodynamic factor to control the crystalline structure of BFO phase and CFO pillar size, which then affect the physical properties and further its practical applications. For instance, we can control the size of the CFO pillar using a temperature substrate to find appropriate spin magnetic switching in the CFO pillar for memory device applications. This study also sheds light on the relationship between thermodynamics and elastic strain energy on the formation of self-assembled matrix-pillars of the BFO-CFO VAN which is important for device fabrication. [ABSTRACT FROM AUTHOR]

The rich physical properties unveiled in a plethora of transition and rare-earth metal oxides have been attributed to the intricate interplays between the orbital, charge, and spin degrees of freedom. Among them, rare-earth manganites (RMnO3) have been attracting tremendous attention owing to the ionic size-induced lattice distortion dictated by the Goldschmidt tolerance factor and the substantial Jahn–Teller distortion unique to Mn3+ ions, which evidently have resulted in a variety of emergent characteristics in electronic, magnetic, and orbital ordering. In this work, we deliberately engineered the orientation of a series of orthorhombic YMnO3 (o-YMO) films grown on SrTiO3(100) [STO(100)] and SrTiO3(110) [STO(110)] substrates by means of pulsed laser deposition. The x-ray diffraction (XRD) and reciprocal space mapping revealed that o-YMO/STO(100) is c-axis-oriented and o-YMO/STO(110) is a-axis-oriented, respectively. The XRD ϕ-scans further indicate that both films have excellent in-plane crystallinity, allowing the exploration of anisotropies along the respective crystallographic orientations. Indeed, the x-ray absorption linear dichroism spectroscopy taken along the respective crystallographic orientations evidently exhibited substantial anisotropy. Theoretical fitting with configuration interaction cluster calculations suggests that the d 3 z 2 − r 2 orbitals are parallel to YMO[001]/(100), leading to stronger electron scattering along the c-axis. Independent polarization-dependent Δ R/R spectra obtained using the femtosecond pump–probe method exhibited substantial anisotropic behaviors in carrier relaxation dynamics when probing along different crystallographic orientations, presumably due to orbital ordering anisotropies. [ABSTRACT FROM AUTHOR]

Hydrogen peroxide (H2O2) production by the electrochemical 2‐electron oxygen reduction reaction (2e− ORR) is a promising alternative to the energy‐intensive anthraquinone process, and single‐atom electrocatalysts show the unique capability of high selectivity toward 2e− ORR against the 4e− one. The extremely low surface density of the single‐atom sites and the inflexibility in manipulating their geometric/electronic configurations, however, compromise the H2O2 yield and impede further performance enhancement. Herein, we construct a family of multiatom catalysts (MACs), on which two or three single atoms are closely coordinated to form high‐density active sites that are versatile in their atomic configurations for optimal adsorption of essential *OOH species. Among them, the Cox–Ni MAC presents excellent electrocatalytic performance for 2e− ORR, in terms of its exceptionally high H2O2 yield in acidic electrolytes (28.96 mol L−1 gcat.−1 h−1) and high selectivity under acidic to neutral conditions in a wide potential region (>80%, 0–0.7 V). Operando X‐ray absorption and density functional theory analyses jointly unveil its unique trimetallic Co2NiN8 configuration, which efficiently induces an appropriate Ni–d orbital filling and modulates the *OOH adsorption, together boosting the electrocatalytic 2e− ORR capability. This work thus provides a new MAC strategy for tuning the geometric/electronic structure of active sites for 2e− ORR and other potential electrochemical processes. [ABSTRACT FROM AUTHOR]

In this study, samarium (Sm-10at%)-doped BiFeO3 (SmBFO) thin films were grown on platinum-coated glass substrates using pulsed laser deposition (PLD) to unveil the correlation between the microstructures and nanomechanical properties of the films. The PLD-derived SmBFO thin films were prepared under various oxygen partial pressures (PO2) of 10, 30, and 50 mTorr at a substrate temperature of 600 °C. The scanning electron microscopy analyses revealed a surface morphology consisting of densely packed grains, although the size distribution varied with the PO2. X-ray diffraction results indicate that all SmBFO thin films are textured and preferentially oriented along the (110) crystallographic orientation. The crystallite sizes of the obtained SmBFO thin films calculated from the Scherrer and (Williamson–Hall) equations increased from 20 (33) nm to 25 (52) nm with increasing PO2. In addition, the nanomechanical properties (the hardness and Young's modulus) of the SmBFO thin films were measured by using nanoindentation. The relationship between the hardness and crystalline size of SmBFO thin films appears to closely follow the Hall–Petch equation. In addition, the PO2 dependence of the film microstructure, the crystallite size, the hardness, and Young's modulus of SmBFO thin films are discussed. [ABSTRACT FROM AUTHOR]

The search for materials for next-generation spintronic applications has witnessed exponentially increasing interest, mainly due to the explosive development of numerous two-dimensional (2D) materials discovered in the last decade. Among them, MXenes have emerged as promising candidates for many applications due to their unique and versatile tunability in structure and properties. In particular, their excellent combination of conductivity and highly charged surfaces leads to outstanding electrochemical properties that are significant in electronic applications. Moreover, the ease of modifying the atomic and electronic structures, and thus the functionalities of MXenes, further opens up the opportunity to realize MXenes-based spintronic device applications. The explosive development of MXenes, such as tuning the bandgap and enhancing their magnetic properties, could pave the way for the integration of MXenes in device configurations suitable for spintronics. In this article, we provide an overview of the potential applications of MXenes with a special focus on spintronic device applications. We commence the discussion with various fundamental aspects of spintronics, including the understanding of materials for spintronics in general, MXenes, and their fabrication, followed by presenting perspectives on plausible strategies and future challenges in integrating MXenes into spintronic devices. [ABSTRACT FROM AUTHOR]

Magnetic spinel oxides have attracted extensive research interest due to their rich physics and wide range of applications. However, these materials invariably suffer suppressed magnetization, due to structural imperfections (e.g., disorder, anti‐site defects, etc.). Herein, a dramatic enhanced magnetization is obtained with an increasement of 5 µB/u.c in CoFe2O4 (CFO) through ionic liquid gating induced hydrogen doping. The intercalated hydrogen ions lead to both distinct lattice expansion of ≈0.7% and notable Fe valence state reduction through electron doping, in which ≈17% Fe3+ is reduced into Fe2+. These facts collectively trigger a site‐specific spin‐flip on tetrahedrally coordinated Co2+ sites that enhances the net ferrimagnetic moment nearly to its theoretical maximum for perfect CFO. [ABSTRACT FROM AUTHOR]

This work reports molecular beam epitaxy (MBE) of two-dimensional (2D) GaSe1−xTex ternary alloys that have recently attracted a lot of interest in physics for prospective electronics and optoelectronics even though they face crucial challenges in their epitaxial technology. Disregarding a distinction in crystal phase symmetry of two end-terminals, i.e., hexagonal-GaSe (h-GaSe) and monoclinic-GaTe (m-GaTe), the majority of hexagonal-GaSe1−xTex (h-GaSe1−xTex) phase on a GaN/sapphire platform is guaranteed under our specific growth conditions without a visible sign of phase transition. We have also proposed extracting the Te composition of the ternary alloy via the experimental in-plane lattice constant, which is consistent with those indicated from energy dispersion X-ray data. Fascinatingly, the experimental and predictable band emission versus Te content displays a continuous redshift from 1.78 eV (h-GaSe) to 1.25 eV (h-GaSe0.4Te0.6) then a reversible blueshift to 1.46 eV (h-GaTe). Importantly, benefiting from the presence of Te incorporated atoms, the photoresponse performance of the hexagonal ternary alloy has greatly enhanced in comparison to the h-GaSe binary in terms of photocurrent density (up to 1250 nA cm−2 for h-GaSe0.65Te0.35 at only 300 mV bias). Overall, the results pave a way for phase/physical engineering of the alloys through the MBE process and realizing self-powered wafer-scale photodetectors based on 2D Ga-based monochalcogenide epitaxial thin films. [ABSTRACT FROM AUTHOR]

In this study, the nanoindentation responses of Bi2Se3 thin film were quantitatively analyzed and simulated by using the finite element method (FEM). The hardness and Young's modulus of Bi2Se3 thin films were experimentally determined using the continuous contact stiffness measurements option built into a Berkovich nanoindenter. Concurrently, FEM was conducted to establish a model describing the contact mechanics at the film/substrate interface, which was then used to reproduce the nanoindentation load-depth and hardness-depth curves. As such, the appropriate material parameters were obtained by correlating the FEM results with the corresponding experimental load-displacement curves. Moreover, the detailed nanoindentation-induced stress distribution in the vicinity around the interface of Bi2Se3 thin film and c-plane sapphires was mapped by FEM simulation for three different indenters, namely, the Berkovich, spherical and flat punch indenters. The results indicated that the nanoindentation-induced stress distribution at the film/substrate interface is indeed strongly dependent on the indenter's geometric shape. [ABSTRACT FROM AUTHOR]

The correlations among microstructure, surface morphology, hardness, and elastic modulus of Bi2Te3 thin films deposited on c-plane sapphire substrates by pulsed laser deposition are investigated. X-ray diffraction (XRD) and transmission electron microscopy are used to characterize the microstructures of the Bi2Te3 thin films. The XRD analyses revealed that the Bi2Te3 thin films were highly (00l)-oriented and exhibited progressively improved crystallinity when the substrate temperature (TS) increased. The hardness and elastic modulus of the Bi2Te3 thin films determined by nanoindentation operated with the continuous contact stiffness measurement (CSM) mode are both substantially larger than those reported for bulk samples, albeit both decrease monotonically with increasing crystallite size and follow the Hall—Petch relation closely. Moreover, the Berkovich nanoindentation-induced crack exhibited trans-granular cracking behaviors for all films investigated. The fracture toughness was significantly higher for films deposited at the lower TS; meanwhile, the fracture energy was almost the same when the crystallite size was suppressed, which indicated a prominent role of grain boundary in governing the deformation characteristics of the present Bi2Te3 films. [ABSTRACT FROM AUTHOR]

The rational design of advanced catalysts for sodium-sulfur (Na-S) batteries is important but remains challenging due to the limited understanding of sulfur catalytic mechanisms. Here, we propose an efficient sulfur host consisting of atomic low-coordinated Zn-N 2 sites dispersed on N-rich microporous graphene (Zn-N 2 @NG), which realizes state-of-the-art sodium-storage performance with a high sulfur content of 66 wt %, high-rate capability (467 mA h g -1 at 5 A g -1 ), and long cycling stability for 6500 cycles with an ultralow capacity decay rate of 0.0062% per cycle. Ex situ methods combined with theoretical calculations demonstrate the superior bidirectional catalysis of Zn-N 2 sites on sulfur conversion (S 8 ↔ Na 2 S). Furthermore, in situ transmission electron microscopy was applied to visualize the microscopic S redox evolution under the catalysis of Zn-N 2 sites without liquid electrolytes. During the sodiation process, both surface S nanoparticles and S molecules in the mircopores of Zn-N 2 @NG quickly convert into Na 2 S nanograins. During the following desodiation process, only a small part of the above Na 2 S can be oxidized into Na 2 S x . These results reveal that, without liquid electrolytes, Na 2 S is difficult to be decomposed even with the assistance of Zn-N 2 sites. This conclusion emphasizes the critical role of liquid electrolytes in the catalytic oxidation of Na 2 S, which was usually ignored by previous works.